Molecular cloning, complete nucleotide sequence, and gene structure of the provirus genome of a retrovirus produced in a human lymphoblastoid cell line
We found and characterized a type D retrovirus produced in a human lymphoblastoid cell line of B-cell lineage. The amino acid sequence of the N-terminal region of the purified major structural protein (PVTRSQGQVSSNTTGRASPHPDTHTIPE) revealed no high homology with any of the known retroviral amino aci...
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Veröffentlicht in: | Virology (New York, N.Y.) N.Y.), 1988-12, Vol.167 (2), p.468-476 |
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container_title | Virology (New York, N.Y.) |
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creator | Oda, Takuzo Ikeda, Shogo Watanabe, Sekiko Hatsushika, Masao Akiyama, Kosuke Mitsunobu, Fumihiro |
description | We found and characterized a type D retrovirus produced in a human lymphoblastoid cell line of B-cell lineage. The amino acid sequence of the N-terminal region of the purified major structural protein (PVTRSQGQVSSNTTGRASPHPDTHTIPE) revealed no high homology with any of the known retroviral amino acid sequences. We have cloned cDNA and the proviral genome integrated in the retrovirus-producing cells, and determined the complete nucleotide sequence and gene structures of the genome. The provirus genome is 8785 by long and has the structure of LTR-
gag-prt-pol-env-LTR. The nucleotide sequences of the long terminal repeat (LTR) region and a part of the
pol gene were closely related to the available sequences of squirrel monkey retrovirus (SMRV), and we designated this virus SMRV
HLB, abbreviated as SMRV-H. The primer (tRNA
1,2
Lys)-binding sequence of SMRV-H (TGGCGCCCA
GGACGTGGGGCTCGA) has a
GG insertion, which is different from that of SMRV. The transmembrane protein of the 3′ terminal region of
env gene contains an amino acid sequence of an immunosuppressive peptide (EVVLQNRRGLDLLTAEQGGICLALQE
RCCFYANKS), in which
R is unique in SMRV-H. The core sequence of the glucocorticoid regulatory element is found upstream of the two 42-bp imperfect repeats in the LTR. Sequences partially homologous to those of the rat IgE-binding protein gene are in gag and pol genes. |
doi_str_mv | 10.1016/0042-6822(88)90109-2 |
format | Article |
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gag-prt-pol-env-LTR. The nucleotide sequences of the long terminal repeat (LTR) region and a part of the
pol gene were closely related to the available sequences of squirrel monkey retrovirus (SMRV), and we designated this virus SMRV
HLB, abbreviated as SMRV-H. The primer (tRNA
1,2
Lys)-binding sequence of SMRV-H (TGGCGCCCA
GGACGTGGGGCTCGA) has a
GG insertion, which is different from that of SMRV. The transmembrane protein of the 3′ terminal region of
env gene contains an amino acid sequence of an immunosuppressive peptide (EVVLQNRRGLDLLTAEQGGICLALQE
RCCFYANKS), in which
R is unique in SMRV-H. The core sequence of the glucocorticoid regulatory element is found upstream of the two 42-bp imperfect repeats in the LTR. Sequences partially homologous to those of the rat IgE-binding protein gene are in gag and pol genes.</description><identifier>ISSN: 0042-6822</identifier><identifier>EISSN: 1096-0341</identifier><identifier>DOI: 10.1016/0042-6822(88)90109-2</identifier><identifier>PMID: 3201749</identifier><identifier>CODEN: VIRLAX</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Amino Acid Sequence ; Base Sequence ; Biological and medical sciences ; Cell Line ; Cloning, Molecular ; DNA - genetics ; Fundamental and applied biological sciences. Psychology ; Genes, Viral ; Genes. Genome ; Lymphocytes - microbiology ; Molecular and cellular biology ; Molecular genetics ; Molecular Sequence Data ; Restriction Mapping ; Retroviridae - genetics ; Retroviridae Proteins - genetics</subject><ispartof>Virology (New York, N.Y.), 1988-12, Vol.167 (2), p.468-476</ispartof><rights>1988 Academic Press, Inc.</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-621bf83ef91e8e38477f506888d7b375dc1e69bf44bb5f2f06c7b5374f5a5e2c3</citedby><cites>FETCH-LOGICAL-c357t-621bf83ef91e8e38477f506888d7b375dc1e69bf44bb5f2f06c7b5374f5a5e2c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0042-6822(88)90109-2$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6828868$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3201749$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oda, Takuzo</creatorcontrib><creatorcontrib>Ikeda, Shogo</creatorcontrib><creatorcontrib>Watanabe, Sekiko</creatorcontrib><creatorcontrib>Hatsushika, Masao</creatorcontrib><creatorcontrib>Akiyama, Kosuke</creatorcontrib><creatorcontrib>Mitsunobu, Fumihiro</creatorcontrib><title>Molecular cloning, complete nucleotide sequence, and gene structure of the provirus genome of a retrovirus produced in a human lymphoblastoid cell line</title><title>Virology (New York, N.Y.)</title><addtitle>Virology</addtitle><description>We found and characterized a type D retrovirus produced in a human lymphoblastoid cell line of B-cell lineage. The amino acid sequence of the N-terminal region of the purified major structural protein (PVTRSQGQVSSNTTGRASPHPDTHTIPE) revealed no high homology with any of the known retroviral amino acid sequences. We have cloned cDNA and the proviral genome integrated in the retrovirus-producing cells, and determined the complete nucleotide sequence and gene structures of the genome. The provirus genome is 8785 by long and has the structure of LTR-
gag-prt-pol-env-LTR. The nucleotide sequences of the long terminal repeat (LTR) region and a part of the
pol gene were closely related to the available sequences of squirrel monkey retrovirus (SMRV), and we designated this virus SMRV
HLB, abbreviated as SMRV-H. The primer (tRNA
1,2
Lys)-binding sequence of SMRV-H (TGGCGCCCA
GGACGTGGGGCTCGA) has a
GG insertion, which is different from that of SMRV. The transmembrane protein of the 3′ terminal region of
env gene contains an amino acid sequence of an immunosuppressive peptide (EVVLQNRRGLDLLTAEQGGICLALQE
RCCFYANKS), in which
R is unique in SMRV-H. The core sequence of the glucocorticoid regulatory element is found upstream of the two 42-bp imperfect repeats in the LTR. Sequences partially homologous to those of the rat IgE-binding protein gene are in gag and pol genes.</description><subject>Amino Acid Sequence</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Cloning, Molecular</subject><subject>DNA - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes, Viral</subject><subject>Genes. Genome</subject><subject>Lymphocytes - microbiology</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Molecular Sequence Data</subject><subject>Restriction Mapping</subject><subject>Retroviridae - genetics</subject><subject>Retroviridae Proteins - genetics</subject><issn>0042-6822</issn><issn>1096-0341</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9u1DAQxiNEVZbCG4DkA0IgNeA_cexcKqEKaKVWXOBsOfa4a-TYi51U6pPwujjdZY9wGnm-34y-8dc0rwj-QDDpP2Lc0baXlL6T8v2ACR5a-qTZ1Nq3mHXkabM5Is-a56X8xPUtBD5tThnFRHTDpvl9mwKYJeiMTEjRx7tzZNK0CzADiosJkGZvARX4tUA0cI50tOgOYm3NeTHzkgElh-YtoF1O9z4vZZXT9NjWKMP8t111uxiwyMcqbJdJRxQept02jUGXOXmLDISAgo_wojlxOhR4eahnzY8vn79fXrU3375eX366aQ3jYm57SkYnGbiBgAQm63mO415KacXIBLeGQD-MruvGkTvqcG_EyJnoHNccqGFnzdv93mquXlhmNfmyutAR0lKUkFyKTnT_BQmng-SMVbDbgyanUjI4tct-0vlBEazW4NSailpTUVKqx-AUrWOvD_uXcQJ7HDokVfU3B10Xo4PLOhpfjlhdJ2UvK3axx6B-2r2HrIrxa3DWZzCzssn_28cfnay3DA</recordid><startdate>198812</startdate><enddate>198812</enddate><creator>Oda, Takuzo</creator><creator>Ikeda, Shogo</creator><creator>Watanabe, Sekiko</creator><creator>Hatsushika, Masao</creator><creator>Akiyama, Kosuke</creator><creator>Mitsunobu, Fumihiro</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>198812</creationdate><title>Molecular cloning, complete nucleotide sequence, and gene structure of the provirus genome of a retrovirus produced in a human lymphoblastoid cell line</title><author>Oda, Takuzo ; Ikeda, Shogo ; Watanabe, Sekiko ; Hatsushika, Masao ; Akiyama, Kosuke ; Mitsunobu, Fumihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-621bf83ef91e8e38477f506888d7b375dc1e69bf44bb5f2f06c7b5374f5a5e2c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Amino Acid Sequence</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Cloning, Molecular</topic><topic>DNA - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes, Viral</topic><topic>Genes. Genome</topic><topic>Lymphocytes - microbiology</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Molecular Sequence Data</topic><topic>Restriction Mapping</topic><topic>Retroviridae - genetics</topic><topic>Retroviridae Proteins - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oda, Takuzo</creatorcontrib><creatorcontrib>Ikeda, Shogo</creatorcontrib><creatorcontrib>Watanabe, Sekiko</creatorcontrib><creatorcontrib>Hatsushika, Masao</creatorcontrib><creatorcontrib>Akiyama, Kosuke</creatorcontrib><creatorcontrib>Mitsunobu, Fumihiro</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Virology (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oda, Takuzo</au><au>Ikeda, Shogo</au><au>Watanabe, Sekiko</au><au>Hatsushika, Masao</au><au>Akiyama, Kosuke</au><au>Mitsunobu, Fumihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular cloning, complete nucleotide sequence, and gene structure of the provirus genome of a retrovirus produced in a human lymphoblastoid cell line</atitle><jtitle>Virology (New York, N.Y.)</jtitle><addtitle>Virology</addtitle><date>1988-12</date><risdate>1988</risdate><volume>167</volume><issue>2</issue><spage>468</spage><epage>476</epage><pages>468-476</pages><issn>0042-6822</issn><eissn>1096-0341</eissn><coden>VIRLAX</coden><abstract>We found and characterized a type D retrovirus produced in a human lymphoblastoid cell line of B-cell lineage. The amino acid sequence of the N-terminal region of the purified major structural protein (PVTRSQGQVSSNTTGRASPHPDTHTIPE) revealed no high homology with any of the known retroviral amino acid sequences. We have cloned cDNA and the proviral genome integrated in the retrovirus-producing cells, and determined the complete nucleotide sequence and gene structures of the genome. The provirus genome is 8785 by long and has the structure of LTR-
gag-prt-pol-env-LTR. The nucleotide sequences of the long terminal repeat (LTR) region and a part of the
pol gene were closely related to the available sequences of squirrel monkey retrovirus (SMRV), and we designated this virus SMRV
HLB, abbreviated as SMRV-H. The primer (tRNA
1,2
Lys)-binding sequence of SMRV-H (TGGCGCCCA
GGACGTGGGGCTCGA) has a
GG insertion, which is different from that of SMRV. The transmembrane protein of the 3′ terminal region of
env gene contains an amino acid sequence of an immunosuppressive peptide (EVVLQNRRGLDLLTAEQGGICLALQE
RCCFYANKS), in which
R is unique in SMRV-H. The core sequence of the glucocorticoid regulatory element is found upstream of the two 42-bp imperfect repeats in the LTR. Sequences partially homologous to those of the rat IgE-binding protein gene are in gag and pol genes.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>3201749</pmid><doi>10.1016/0042-6822(88)90109-2</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
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ispartof | Virology (New York, N.Y.), 1988-12, Vol.167 (2), p.468-476 |
issn | 0042-6822 1096-0341 |
language | eng |
recordid | cdi_proquest_miscellaneous_78587474 |
source | MEDLINE; Elsevier ScienceDirect Journals Complete; EZB-FREE-00999 freely available EZB journals |
subjects | Amino Acid Sequence Base Sequence Biological and medical sciences Cell Line Cloning, Molecular DNA - genetics Fundamental and applied biological sciences. Psychology Genes, Viral Genes. Genome Lymphocytes - microbiology Molecular and cellular biology Molecular genetics Molecular Sequence Data Restriction Mapping Retroviridae - genetics Retroviridae Proteins - genetics |
title | Molecular cloning, complete nucleotide sequence, and gene structure of the provirus genome of a retrovirus produced in a human lymphoblastoid cell line |
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